PRORP (protein only RNase P catalytic subunit) - Rat Genome Database

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Gene: PRORP (protein only RNase P catalytic subunit) Homo sapiens
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Symbol: PRORP
Name: protein only RNase P catalytic subunit
RGD ID: 1312913
HGNC Page HGNC:19958
Description: Enables ribonuclease P activity. Involved in mitochondrial tRNA 5'-end processing. Located in mitochondrion and nucleoplasm. Part of mitochondrial ribonuclease P complex. Implicated in combined oxidative phosphorylation deficiency 54.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: COXPD54; KIAA0391; mitochondrial ribonuclease P catalytic subunit; mitochondrial ribonuclease P protein 3; mitochondrial RNase P protein 3; mitochondrial RNase P subunit 3; MRPP3; proteinaceous RNase P
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381435,121,839 - 35,277,622 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1435,121,846 - 35,277,622 (+)EnsemblGRCh38hg38GRCh38
GRCh371435,591,045 - 35,746,828 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361434,661,527 - 34,813,022 (+)NCBINCBI36Build 36hg18NCBI36
Celera1415,455,607 - 15,607,100 (+)NCBICelera
Cytogenetic Map14q13.2NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBIHuRef
CHM1_11435,591,261 - 35,743,020 (+)NCBICHM1_1
T2T-CHM13v2.01429,318,793 - 29,465,226 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9205841   PMID:12477932   PMID:15342556   PMID:16344560   PMID:17114934   PMID:17213182   PMID:18984158   PMID:19624571   PMID:20953189   PMID:21873635   PMID:23042678   PMID:23755257  
PMID:24763589   PMID:25437307   PMID:25953853   PMID:26186194   PMID:26496610   PMID:26687479   PMID:27499296   PMID:28380382   PMID:28514442   PMID:28611215   PMID:28675297   PMID:28700943  
PMID:29395067   PMID:29509190   PMID:29880640   PMID:30572598   PMID:30940648   PMID:31091453   PMID:31240132   PMID:31617661   PMID:31871319   PMID:32344865   PMID:32457219   PMID:32628020  
PMID:32877691   PMID:32994395   PMID:33961781   PMID:34079125   PMID:34373451   PMID:34489609   PMID:34715011   PMID:34800366   PMID:35439318   PMID:35944360   PMID:36114006   PMID:36215168  
PMID:36543142   PMID:37314216   PMID:37558808   PMID:37689310   PMID:38262497  


Genomics

Comparative Map Data
PRORP
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381435,121,839 - 35,277,622 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1435,121,846 - 35,277,622 (+)EnsemblGRCh38hg38GRCh38
GRCh371435,591,045 - 35,746,828 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361434,661,527 - 34,813,022 (+)NCBINCBI36Build 36hg18NCBI36
Celera1415,455,607 - 15,607,100 (+)NCBICelera
Cytogenetic Map14q13.2NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBIHuRef
CHM1_11435,591,261 - 35,743,020 (+)NCBICHM1_1
T2T-CHM13v2.01429,318,793 - 29,465,226 (+)NCBIT2T-CHM13v2.0
Prorp
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391255,349,422 - 55,429,276 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1255,346,362 - 55,429,318 (+)EnsemblGRCm39 Ensembl
GRCm381255,302,637 - 55,382,492 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1255,299,577 - 55,382,533 (+)EnsemblGRCm38mm10GRCm38
MGSCv371256,403,624 - 56,483,478 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361256,220,753 - 56,300,617 (+)NCBIMGSCv36mm8
Celera1256,446,616 - 56,531,738 (+)NCBICelera
Cytogenetic Map12C1NCBI
cM Map1223.91NCBI
Prorp
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8678,404,821 - 78,497,562 (+)NCBIGRCr8
mRatBN7.2672,669,659 - 72,762,419 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl672,670,847 - 72,762,416 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx673,093,590 - 73,182,668 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0673,399,942 - 73,489,024 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0672,828,549 - 72,917,703 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0676,079,880 - 76,171,298 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl676,079,880 - 76,171,296 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0685,614,276 - 85,708,817 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4675,539,870 - 75,633,118 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1675,543,495 - 75,636,184 (+)NCBI
Celera671,512,144 - 71,602,932 (+)NCBICelera
Cytogenetic Map6q23NCBI
Prorp
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540925,791,575 - 25,920,077 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540925,791,209 - 25,920,651 (-)NCBIChiLan1.0ChiLan1.0
PRORP
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21536,432,152 - 36,590,190 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11435,648,655 - 35,808,108 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01415,871,707 - 16,027,634 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11434,056,234 - 34,209,657 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1434,056,620 - 34,209,657 (+)Ensemblpanpan1.1panPan2
PRORP
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1813,885,734 - 14,007,224 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha813,681,902 - 13,803,857 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0813,991,929 - 14,113,298 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl813,992,144 - 14,113,292 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1813,693,596 - 13,814,946 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0813,758,157 - 13,879,746 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0814,047,450 - 14,169,639 (+)NCBIUU_Cfam_GSD_1.0
Prorp
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864045,776,936 - 45,908,465 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049364949,282,894 - 9,414,350 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PRORP
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl764,620,517 - 64,762,428 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1764,620,514 - 64,763,272 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2769,530,089 - 69,535,675 (-)NCBISscrofa10.2Sscrofa10.2susScr3
PRORP
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12411,936,410 - 12,081,721 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2411,936,410 - 12,083,519 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666053897,654 - 1,044,936 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in PRORP
57 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1 copy number loss See cases [RCV000051485] Chr14:20196945..45284802 [GRCh38]
Chr14:20665104..45754005 [GRCh37]
Chr14:19734944..44823755 [NCBI36]
Chr14:14q11.2-21.2		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:23548960-41983402)x1 copy number loss See cases [RCV000051490] Chr14:23548960..41983402 [GRCh38]
Chr14:24018169..42452605 [GRCh37]
Chr14:23088009..41522355 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
GRCh38/hg38 14q13.1-13.3(chr14:34450934-36880151)x1 copy number loss See cases [RCV000051492] Chr14:34450934..36880151 [GRCh38]
Chr14:34920140..37349356 [GRCh37]
Chr14:33989891..36419107 [NCBI36]
Chr14:14q13.1-13.3		 pathogenic
GRCh38/hg38 14q12-21.2(chr14:30670314-44990595)x3 copy number gain See cases [RCV000052292] Chr14:30670314..44990595 [GRCh38]
Chr14:31139520..45459798 [GRCh37]
Chr14:30209271..44529548 [NCBI36]
Chr14:14q12-21.2		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3 copy number gain See cases [RCV000053803] Chr14:20000611..38984415 [GRCh38]
Chr14:20468770..39453619 [GRCh37]
Chr14:19538610..38523370 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20150949-39746154)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|See cases [RCV000053806] Chr14:20150949..39746154 [GRCh38]
Chr14:20619108..40215358 [GRCh37]
Chr14:19688948..39285109 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
NM_001256678.1(KIAA0391):c.1228-38564G>A single nucleotide variant Lung cancer [RCV000098720] Chr14:35228163 [GRCh38]
Chr14:35697369 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh38/hg38 14q12-21.1(chr14:30382554-37712341)x1 copy number loss See cases [RCV000135334] Chr14:30382554..37712341 [GRCh38]
Chr14:30851760..38181546 [GRCh37]
Chr14:29921511..37251297 [NCBI36]
Chr14:14q12-21.1		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q13.2-21.2(chr14:35068276-43994777)x1 copy number loss See cases [RCV000137841] Chr14:35068276..43994777 [GRCh38]
Chr14:35537482..44463980 [GRCh37]
Chr14:34607233..43533730 [NCBI36]
Chr14:14q13.2-21.2		 pathogenic
GRCh38/hg38 14q13.2(chr14:35068276-35231604)x3 copy number gain See cases [RCV000139964] Chr14:35068276..35231604 [GRCh38]
Chr14:35537482..35700810 [GRCh37]
Chr14:34607233..34770561 [NCBI36]
Chr14:14q13.2		 likely benign
GRCh38/hg38 14q13.1-21.1(chr14:33880412-42359485)x1 copy number loss See cases [RCV000142211] Chr14:33880412..42359485 [GRCh38]
Chr14:34349618..42828688 [GRCh37]
Chr14:33419369..41898438 [NCBI36]
Chr14:14q13.1-21.1		 pathogenic
GRCh38/hg38 14q12-21.2(chr14:30792271-44685131)x1 copy number loss See cases [RCV000143063] Chr14:30792271..44685131 [GRCh38]
Chr14:31261477..45154334 [GRCh37]
Chr14:30331228..44224084 [NCBI36]
Chr14:14q12-21.2		 pathogenic
GRCh38/hg38 14q13.1-13.3(chr14:33762166-36191750)x1 copy number loss See cases [RCV000142534] Chr14:33762166..36191750 [GRCh38]
Chr14:34231372..36660956 [GRCh37]
Chr14:33301123..35730707 [NCBI36]
Chr14:14q13.1-13.3		 uncertain significance
GRCh38/hg38 14q13.2(chr14:35109816-35151026)x1 copy number loss See cases [RCV000142699] Chr14:35109816..35151026 [GRCh38]
Chr14:35579022..35620232 [GRCh37]
Chr14:34648773..34689983 [NCBI36]
Chr14:14q13.2		 benign
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3 copy number gain See cases [RCV000143186] Chr14:20022693..44093672 [GRCh38]
Chr14:20490852..44562875 [GRCh37]
Chr14:19560692..43632625 [NCBI36]
Chr14:14q11.2-21.2		 pathogenic
GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3 copy number gain See cases [RCV000143748] Chr14:20043513..48642042 [GRCh38]
Chr14:20511672..49111245 [GRCh37]
Chr14:19581512..48180995 [NCBI36]
Chr14:14q11.2-21.3		 pathogenic
GRCh37/hg19 14q11.2-22.2(chr14:23164384-54733411)x3 copy number gain See cases [RCV000447658] Chr14:23164384..54733411 [GRCh37]
Chr14:14q11.2-22.2		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q13.2(chr14:35734798-35784055)x3 copy number gain See cases [RCV000445791] Chr14:35734798..35784055 [GRCh37]
Chr14:14q13.2		 conflicting data from submitters
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
NM_014672.4(PRORP):c.1333C>T (p.Arg445Trp) single nucleotide variant not specified [RCV004288981] Chr14:35266784 [GRCh38]
Chr14:35735990 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.426T>G (p.Ser142Arg) single nucleotide variant not specified [RCV004324194] Chr14:35123671 [GRCh38]
Chr14:35592877 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.1201C>T (p.Arg401Cys) single nucleotide variant not specified [RCV004317572] Chr14:35180703 [GRCh38]
Chr14:35649909 [GRCh37]
Chr14:14q13.2		 likely benign
GRCh37/hg19 14q13.1-13.2(chr14:35232984-35652742)x3 copy number gain not provided [RCV000683606] Chr14:35232984..35652742 [GRCh37]
Chr14:14q13.1-13.2		 uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q13.2(chr14:35592538-35613784)x1 copy number loss not provided [RCV000750968] Chr14:35592538..35613784 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35595938-35613784)x1 copy number loss not provided [RCV000750969] Chr14:35595938..35613784 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35602956-35613619)x1 copy number loss not provided [RCV000750970] Chr14:35602956..35613619 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35602956-35613784)x1 copy number loss not provided [RCV000750971] Chr14:35602956..35613784 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35602956-35614319)x0 copy number loss not provided [RCV000750972] Chr14:35602956..35614319 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35665374-35702800)x0 copy number loss not provided [RCV000750973] Chr14:35665374..35702800 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35702299-35702800)x1 copy number loss not provided [RCV000750974] Chr14:35702299..35702800 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35702299-35703521)x1 copy number loss not provided [RCV000750975] Chr14:35702299..35703521 [GRCh37]
Chr14:14q13.2		 benign
GRCh37/hg19 14q13.2(chr14:35702299-35717282)x1 copy number loss not provided [RCV000750976] Chr14:35702299..35717282 [GRCh37]
Chr14:14q13.2		 benign
NM_014672.4(PRORP):c.1454C>T (p.Ala485Val) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV001824882]|Perrault syndrome 1 [RCV000855453] Chr14:35270430 [GRCh38]
Chr14:35739636 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic
NM_014672.4(PRORP):c.1197dup (p.Ser400fs) duplication Combined oxidative phosphorylation deficiency 54 [RCV001824884]|Global developmental delay [RCV000855455]|Leukoencephalopathy [RCV001873232] Chr14:35180695..35180696 [GRCh38]
Chr14:35649901..35649902 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic
NM_014672.4(PRORP):c.1334G>A (p.Arg445Gln) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV001824883]|Global developmental delay [RCV000855454]|Leukoencephalopathy [RCV001869241] Chr14:35266785 [GRCh38]
Chr14:35735991 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic
GRCh37/hg19 14q11.2-21.3(chr14:20511672-47481203) copy number gain Seizure [RCV002280625] Chr14:20511672..47481203 [GRCh37]
Chr14:14q11.2-21.3		 pathogenic
GRCh37/hg19 14q13.2(chr14:35724243-35850214)x3 copy number gain not provided [RCV000847927] Chr14:35724243..35850214 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q13.2(chr14:35395019-35783469)x3 copy number gain not provided [RCV001006615] Chr14:35395019..35783469 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q11.2-21.1(chr14:20511672-42881888)x3 copy number gain not provided [RCV001249358] Chr14:20511672..42881888 [GRCh37]
Chr14:14q11.2-21.1		 not provided
NC_000014.8:g.(35596818_35649875)_(35649984_35735932)dup duplication not specified [RCV004783627] Chr14:35649875..35649984 [GRCh37]
Chr14:14q13.2		 uncertain significance
NC_000014.8:g.(?_35182071)_(35873850_?)del deletion Ectodermal dysplasia and immunodeficiency 2 [RCV003107717]|not provided [RCV003113213] Chr14:35182071..35873850 [GRCh37]
Chr14:14q13.1-13.2		 uncertain significance|no classifications from unflagged records
NM_014672.4(PRORP):c.1202G>A (p.Arg401His) single nucleotide variant not specified [RCV004282262] Chr14:35180704 [GRCh38]
Chr14:35649910 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q11.2-21.2(chr14:20511672-44829030)x3 copy number gain not provided [RCV001006605] Chr14:20511672..44829030 [GRCh37]
Chr14:14q11.2-21.2		 pathogenic
GRCh37/hg19 14q13.1-21.2(chr14:33608925-44570367) copy number loss Poor motor coordination [RCV001352634] Chr14:33608925..44570367 [GRCh37]
Chr14:14q13.1-21.2		 pathogenic
NM_014672.4(PRORP):c.1235A>G (p.Asn412Ser) single nucleotide variant Childhood onset sensorineural hearing impairment [RCV001868407]|Combined oxidative phosphorylation deficiency 54 [RCV001825014]|Perrault syndrome 1 [RCV001868406]|not specified [RCV004039969] Chr14:35180737 [GRCh38]
Chr14:35649943 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic|uncertain significance
NM_014672.4(PRORP):c.1301C>A (p.Ala434Asp) single nucleotide variant Childhood onset sensorineural hearing impairment [RCV001868408]|Combined oxidative phosphorylation deficiency 54 [RCV001825015]|PRORP-related disorder [RCV003941102] Chr14:35266752 [GRCh38]
Chr14:35735958 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic|benign
NM_014672.4(PRORP):c.1261C>T (p.Arg421Cys) single nucleotide variant Leukoencephalopathy [RCV001868409]|not specified [RCV004039970] Chr14:35180763 [GRCh38]
Chr14:35649969 [GRCh37]
Chr14:14q13.2		 likely pathogenic|uncertain significance
NM_017917.4(PPP2R3C):c.-9A>G single nucleotide variant Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy [RCV001789587]|PPP2R3C-related disorder [RCV003984106]|Spermatogenic failure 36 [RCV001789588]|not provided [RCV004715552] Chr14:35121968 [GRCh38]
Chr14:35591174 [GRCh37]
Chr14:14q13.2		 benign
NM_014672.4(PRORP):c.16_19del (p.Phe6fs) microsatellite not specified [RCV002248135] Chr14:35123257..35123260 [GRCh38]
Chr14:35592463..35592466 [GRCh37]
Chr14:14q13.2		 uncertain significance
NC_000014.8:g.(21162263_36986276)_(36987308_50713602)del deletion Brain-lung-thyroid syndrome [RCV002221171] Chr14:36986276..36987308 [GRCh37]
Chr14:14q11.2-21.3		 pathogenic
NM_014672.4(PRORP):c.1505G>A (p.Arg502Gln) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV002283719] Chr14:35270481 [GRCh38]
Chr14:35739687 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q13.1-13.3(chr14:34904407-36784136)x1 copy number loss not provided [RCV002511791] Chr14:34904407..36784136 [GRCh37]
Chr14:14q13.1-13.3		 pathogenic
NM_014672.4(PRORP):c.1241C>T (p.Ala414Val) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV002510555] Chr14:35180743 [GRCh38]
Chr14:35649949 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic
NM_014672.4(PRORP):c.1093T>C (p.Tyr365His) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV002510556] Chr14:35127537 [GRCh38]
Chr14:35596743 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1159A>G (p.Thr387Ala) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV002510554] Chr14:35127603 [GRCh38]
Chr14:35596809 [GRCh37]
Chr14:14q13.2		 pathogenic|likely pathogenic
NM_014672.4(PRORP):c.437C>T (p.Ser146Leu) single nucleotide variant not specified [RCV004265679] Chr14:35123682 [GRCh38]
Chr14:35592888 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.703G>A (p.Asp235Asn) single nucleotide variant not specified [RCV004306584] Chr14:35123948 [GRCh38]
Chr14:35593154 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_017917.4(PPP2R3C):c.38C>T (p.Thr13Met) single nucleotide variant not specified [RCV004356400] Chr14:35121922 [GRCh38]
Chr14:35591128 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1475A>C (p.His492Pro) single nucleotide variant not specified [RCV004357242] Chr14:35270451 [GRCh38]
Chr14:35739657 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1380G>A (p.Met460Ile) single nucleotide variant not specified [RCV004337974] Chr14:35266831 [GRCh38]
Chr14:35736037 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.228G>A (p.Lys76=) single nucleotide variant not provided [RCV003393376] Chr14:35123473 [GRCh38]
Chr14:35592679 [GRCh37]
Chr14:14q13.2		 likely benign
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3 copy number gain not provided [RCV003485022] Chr14:20511673..61826023 [GRCh37]
Chr14:14q11.2-23.1		 pathogenic
GRCh37/hg19 14q13.1-13.3(chr14:34585231-37477843)x1 copy number loss not provided [RCV003483199] Chr14:34585231..37477843 [GRCh37]
Chr14:14q13.1-13.3		 pathogenic
GRCh37/hg19 14q13.2(chr14:35561562-35723514)x1 copy number loss not provided [RCV003483200] Chr14:35561562..35723514 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q13.1-13.2(chr14:35059946-35787671)x3 copy number gain not specified [RCV003987068] Chr14:35059946..35787671 [GRCh37]
Chr14:14q13.1-13.2		 uncertain significance
GRCh37/hg19 14q13.2(chr14:35360640-35936592)x3 copy number gain not specified [RCV003987042] Chr14:35360640..35936592 [GRCh37]
Chr14:14q13.2		 uncertain significance
GRCh37/hg19 14q12-21.2(chr14:29190489-45325177)x1 copy number loss not specified [RCV003987053] Chr14:29190489..45325177 [GRCh37]
Chr14:14q12-21.2		 pathogenic
NM_014672.4(PRORP):c.690G>A (p.Leu230=) single nucleotide variant PRORP-related disorder [RCV003922325] Chr14:35123935 [GRCh38]
Chr14:35593141 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.1002A>G (p.Gln334=) single nucleotide variant PRORP-related disorder [RCV003932147] Chr14:35126750 [GRCh38]
Chr14:35595956 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.686C>T (p.Ala229Val) single nucleotide variant PRORP-related disorder [RCV003933852]|not provided [RCV003992811] Chr14:35123931 [GRCh38]
Chr14:35593137 [GRCh37]
Chr14:14q13.2		 benign|likely benign
NM_014672.4(PRORP):c.1310A>G (p.Asn437Ser) single nucleotide variant PRORP-related disorder [RCV003984534] Chr14:35266761 [GRCh38]
Chr14:35735967 [GRCh37]
Chr14:14q13.2		 benign
NM_014672.4(PRORP):c.176del (p.Thr59fs) deletion Combined oxidative phosphorylation deficiency 54 [RCV003990818] Chr14:35123421 [GRCh38]
Chr14:35592627 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.934C>T (p.Gln312Ter) single nucleotide variant Combined oxidative phosphorylation deficiency 54 [RCV003990795] Chr14:35124179 [GRCh38]
Chr14:35593385 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.161A>G (p.Gln54Arg) single nucleotide variant not specified [RCV004507421] Chr14:35123406 [GRCh38]
Chr14:35592612 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.176C>T (p.Thr59Met) single nucleotide variant not specified [RCV004507422] Chr14:35123421 [GRCh38]
Chr14:35592627 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.266C>G (p.Ala89Gly) single nucleotide variant not specified [RCV004507425] Chr14:35123511 [GRCh38]
Chr14:35592717 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.311C>T (p.Ala104Val) single nucleotide variant not specified [RCV004507426] Chr14:35123556 [GRCh38]
Chr14:35592762 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.39G>C (p.Lys13Asn) single nucleotide variant not specified [RCV004507427] Chr14:35123284 [GRCh38]
Chr14:35592490 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.640A>G (p.Ser214Gly) single nucleotide variant not specified [RCV004507428] Chr14:35123885 [GRCh38]
Chr14:35593091 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.800A>G (p.Tyr267Cys) single nucleotide variant not specified [RCV004507429] Chr14:35124045 [GRCh38]
Chr14:35593251 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.229C>A (p.Gln77Lys) single nucleotide variant not specified [RCV004507423] Chr14:35123474 [GRCh38]
Chr14:35592680 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.250T>G (p.Phe84Val) single nucleotide variant not specified [RCV004507424] Chr14:35123495 [GRCh38]
Chr14:35592701 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.101C>A (p.Ala34Glu) single nucleotide variant not specified [RCV004507411] Chr14:35123346 [GRCh38]
Chr14:35592552 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1022C>T (p.Thr341Ile) single nucleotide variant not specified [RCV004507412] Chr14:35126770 [GRCh38]
Chr14:35595976 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1046C>T (p.Ser349Leu) single nucleotide variant not specified [RCV004507413] Chr14:35127490 [GRCh38]
Chr14:35596696 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.1155G>C (p.Lys385Asn) single nucleotide variant not specified [RCV004507414] Chr14:35127599 [GRCh38]
Chr14:35596805 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1192A>C (p.Ile398Leu) single nucleotide variant not specified [RCV004507415] Chr14:35180694 [GRCh38]
Chr14:35649900 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1319T>C (p.Leu440Pro) single nucleotide variant not specified [RCV004507416] Chr14:35266770 [GRCh38]
Chr14:35735976 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.1375G>A (p.Glu459Lys) single nucleotide variant not specified [RCV004507417] Chr14:35266826 [GRCh38]
Chr14:35736032 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.146A>G (p.Lys49Arg) single nucleotide variant not specified [RCV004507418] Chr14:35123391 [GRCh38]
Chr14:35592597 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.151A>G (p.Met51Val) single nucleotide variant not specified [RCV004507419] Chr14:35123396 [GRCh38]
Chr14:35592602 [GRCh37]
Chr14:14q13.2		 likely benign
NM_014672.4(PRORP):c.155C>T (p.Ser52Phe) single nucleotide variant not specified [RCV004507420] Chr14:35123400 [GRCh38]
Chr14:35592606 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.391T>G (p.Leu131Val) single nucleotide variant not specified [RCV004660347] Chr14:35123636 [GRCh38]
Chr14:35592842 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.184A>G (p.Ile62Val) single nucleotide variant not specified [RCV004648829] Chr14:35123429 [GRCh38]
Chr14:35592635 [GRCh37]
Chr14:14q13.2		 uncertain significance
NM_014672.4(PRORP):c.187G>A (p.Ala63Thr) single nucleotide variant not specified [RCV004648830] Chr14:35123432 [GRCh38]
Chr14:35592638 [GRCh37]
Chr14:14q13.2		 uncertain significance
NC_000014.8:g.(35739803_35742640)_(35746829_?)dup duplication not specified [RCV004702726] Chr14:35742640..35746829 [GRCh37]
Chr14:14q13.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2365
Count of miRNA genes:796
Interacting mature miRNAs:917
Transcripts:ENST00000250377, ENST00000321130, ENST00000534898, ENST00000557404, ENST00000557565, ENST00000603544, ENST00000603588, ENST00000603611, ENST00000604073, ENST00000604948, ENST00000605201, ENST00000605870
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407159292GWAS808268_Hlean body mass QTL GWAS808268 (human)2e-08body lean mass (VT:0010483)total body lean mass (CMO:0003950)143520426435204265Human
407234988GWAS883964_Hgranulocyte percentage of myeloid white cells QTL GWAS883964 (human)2e-10granulocyte percentage of myeloid white cells143513081635130817Human
407146669GWAS795645_Hpsoriasis QTL GWAS795645 (human)4e-09psoriasis143521296635212967Human
407129803GWAS778779_Hpsoriasis QTL GWAS778779 (human)2e-08psoriasis143521296635212967Human

Markers in Region
D10S577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371099,071,763 - 99,071,977UniSTSGRCh37
Build 361099,061,753 - 99,061,967RGDNCBI36
Celera1092,810,245 - 92,810,447RGD
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map14q13.2UniSTS
HuRef1079,924,120 - 79,924,538UniSTS
HuRef1092,697,481 - 92,697,679UniSTS
Marshfield Genetic Map10118.94RGD
Marshfield Genetic Map10118.94UniSTS
Genethon Genetic Map10126.1UniSTS
GeneMap99-GB4 RH Map10459.97UniSTS
Whitehead-YAC Contig Map10 UniSTS
NCBI RH Map101071.9UniSTS
D14S1014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,620,702 - 35,620,943UniSTSGRCh37
Build 361434,690,453 - 34,690,694RGDNCBI36
Celera1415,484,532 - 15,484,773RGD
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map14q13UniSTS
Cytogenetic Map14qUniSTS
HuRef1415,733,828 - 15,734,065UniSTS
Marshfield Genetic Map1442.81UniSTS
Marshfield Genetic Map1442.81RGD
Genethon Genetic Map1435.3UniSTS
TNG Radiation Hybrid Map148108.0UniSTS
deCODE Assembly Map1438.13UniSTS
Whitehead-YAC Contig Map14 UniSTS
SHGC-104644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,693,956 - 35,694,256UniSTSGRCh37
Build 361434,763,707 - 34,764,007RGDNCBI36
Celera1415,557,781 - 15,558,081RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,807,094 - 15,807,394UniSTS
TNG Radiation Hybrid Map148035.0UniSTS
G36298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,737,572 - 35,737,678UniSTSGRCh37
Build 361434,807,323 - 34,807,429RGDNCBI36
Celera1415,601,401 - 15,601,507RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,851,926 - 15,852,032UniSTS
G36079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,723,402 - 35,723,572UniSTSGRCh37
Build 361434,793,153 - 34,793,323RGDNCBI36
Celera1415,587,232 - 15,587,402RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,837,758 - 15,837,928UniSTS
D14S1289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,623,754 - 35,623,902UniSTSGRCh37
Build 361434,693,505 - 34,693,653RGDNCBI36
Celera1415,487,588 - 15,487,736RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,736,880 - 15,737,028UniSTS
G36006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,724,183 - 35,724,326UniSTSGRCh37
Build 361434,793,934 - 34,794,077RGDNCBI36
Celera1415,588,013 - 15,588,156RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,838,539 - 15,838,682UniSTS
G35479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,605,404 - 35,605,544UniSTSGRCh37
Build 361434,675,155 - 34,675,295RGDNCBI36
Celera1415,469,234 - 15,469,374RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,718,530 - 15,718,670UniSTS
G35869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,677,398 - 35,677,524UniSTSGRCh37
Build 361434,747,149 - 34,747,275RGDNCBI36
Celera1415,541,224 - 15,541,350RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,790,535 - 15,790,661UniSTS
G35684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,618,812 - 35,619,030UniSTSGRCh37
Build 361434,688,563 - 34,688,781RGDNCBI36
Celera1415,482,642 - 15,482,860RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,731,938 - 15,732,156UniSTS
G35748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371435,722,660 - 35,722,812UniSTSGRCh37
Build 361434,792,411 - 34,792,563RGDNCBI36
Celera1415,586,490 - 15,586,642RGD
Cytogenetic Map14q13.2UniSTS
HuRef1415,837,016 - 15,837,168UniSTS
GDB:631802  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map3q21-q22UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.22-p11.21UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map2q21UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map20p11.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map2p24.1UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS
RH47252  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q13.2UniSTS
GeneMap99-GB4 RH Map1468.38UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2617 2790 2283 5331 1927 2864 10 764 2536 609 2490 8447 7132 103 3881 1 1140 2038 1963 184 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001256678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001414503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA838769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB002389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI431599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC044580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP373829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ063741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX161394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX161487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX760644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA459368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC404874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DT217089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455861 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000250377   ⟹   ENSP00000250377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,564 - 35,277,614 (+)Ensembl
Ensembl Acc Id: ENST00000321130   ⟹   ENSP00000324697
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,552 - 35,274,078 (+)Ensembl
Ensembl Acc Id: ENST00000534898   ⟹   ENSP00000440915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,552 - 35,277,622 (+)Ensembl
Ensembl Acc Id: ENST00000557404   ⟹   ENSP00000450898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,759 - 35,273,485 (+)Ensembl
Ensembl Acc Id: ENST00000557565   ⟹   ENSP00000454657
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,549 - 35,317,474 (+)Ensembl
Ensembl Acc Id: ENST00000603544   ⟹   ENSP00000473856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,677 - 35,273,670 (+)Ensembl
Ensembl Acc Id: ENST00000603588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,121,846 - 35,127,611 (+)Ensembl
Ensembl Acc Id: ENST00000603611   ⟹   ENSP00000474967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,121,846 - 35,123,347 (+)Ensembl
Ensembl Acc Id: ENST00000604073   ⟹   ENSP00000474656
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,303 - 35,123,304 (+)Ensembl
Ensembl Acc Id: ENST00000604948   ⟹   ENSP00000474620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,547 - 35,273,690 (+)Ensembl
Ensembl Acc Id: ENST00000605201   ⟹   ENSP00000474700
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,554 - 35,123,315 (+)Ensembl
Ensembl Acc Id: ENST00000605870   ⟹   ENSP00000474299
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1435,122,722 - 35,274,017 (+)Ensembl
RefSeq Acc Id: NM_001256678   ⟹   NP_001243607
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,277,622 (+)NCBI
GRCh371435,591,527 - 35,743,284 (+)NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBI
CHM1_11435,591,261 - 35,743,020 (+)NCBI
T2T-CHM13v2.01429,319,506 - 29,465,226 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001256679   ⟹   NP_001243608
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,277,622 (+)NCBI
GRCh371435,591,527 - 35,743,284 (+)NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBI
CHM1_11435,591,261 - 35,743,020 (+)NCBI
T2T-CHM13v2.01429,319,506 - 29,465,226 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001256680   ⟹   NP_001243609
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,277,622 (+)NCBI
GRCh371435,591,527 - 35,743,284 (+)NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBI
CHM1_11435,591,492 - 35,743,020 (+)NCBI
T2T-CHM13v2.01429,319,506 - 29,465,226 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001256681   ⟹   NP_001243610
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,277,622 (+)NCBI
GRCh371435,591,527 - 35,743,284 (+)NCBI
HuRef1415,704,222 - 15,857,638 (+)NCBI
CHM1_11435,591,492 - 35,743,020 (+)NCBI
T2T-CHM13v2.01429,319,506 - 29,465,226 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001414503   ⟹   NP_001401432
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,121,839 - 35,274,065 (+)NCBI
T2T-CHM13v2.01429,318,793 - 29,461,669 (+)NCBI
RefSeq Acc Id: NM_014672   ⟹   NP_055487
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,277,622 (+)NCBI
GRCh371435,591,527 - 35,743,284 (+)NCBI
Build 361434,661,527 - 34,813,022 (+)NCBI Archive
Celera1415,455,607 - 15,607,100 (+)RGD
HuRef1415,704,222 - 15,857,638 (+)NCBI
CHM1_11435,591,261 - 35,743,020 (+)NCBI
T2T-CHM13v2.01429,319,506 - 29,465,226 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001243607 (Get FASTA)   NCBI Sequence Viewer  
  NP_001243608 (Get FASTA)   NCBI Sequence Viewer  
  NP_001243609 (Get FASTA)   NCBI Sequence Viewer  
  NP_001243610 (Get FASTA)   NCBI Sequence Viewer  
  NP_001401432 (Get FASTA)   NCBI Sequence Viewer  
  NP_055487 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH32221 (Get FASTA)   NCBI Sequence Viewer  
  AAH44580 (Get FASTA)   NCBI Sequence Viewer  
  BAA20845 (Get FASTA)   NCBI Sequence Viewer  
  BAG63351 (Get FASTA)   NCBI Sequence Viewer  
  BAG64540 (Get FASTA)   NCBI Sequence Viewer  
  BAG64973 (Get FASTA)   NCBI Sequence Viewer  
  CAD61881 (Get FASTA)   NCBI Sequence Viewer  
  CAD61937 (Get FASTA)   NCBI Sequence Viewer  
  EAW65878 (Get FASTA)   NCBI Sequence Viewer  
  EAW65879 (Get FASTA)   NCBI Sequence Viewer  
  EAW65880 (Get FASTA)   NCBI Sequence Viewer  
  EAW65881 (Get FASTA)   NCBI Sequence Viewer  
  EAW65882 (Get FASTA)   NCBI Sequence Viewer  
  EAW65883 (Get FASTA)   NCBI Sequence Viewer  
  EAW65884 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000250377
  ENSP00000250377.8
  ENSP00000324697
  ENSP00000324697.9
  ENSP00000440915
  ENSP00000440915.2
  ENSP00000450898.3
  ENSP00000473856.1
  ENSP00000474299
  ENSP00000474299.1
  ENSP00000474620
  ENSP00000474620.1
  ENSP00000474656.1
  ENSP00000474700.1
  ENSP00000474967.1
GenBank Protein O15091 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_055487   ⟸   NM_014672
- Peptide Label: isoform 1 precursor
- UniProtKB: Q86YB5 (UniProtKB/Swiss-Prot),   Q86SZ4 (UniProtKB/Swiss-Prot),   D3DSA1 (UniProtKB/Swiss-Prot),   D3DS99 (UniProtKB/Swiss-Prot),   C4AM93 (UniProtKB/Swiss-Prot),   B4E211 (UniProtKB/Swiss-Prot),   B4E0S8 (UniProtKB/Swiss-Prot),   B4DXD9 (UniProtKB/Swiss-Prot),   Q8N5L5 (UniProtKB/Swiss-Prot),   O15091 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243607   ⟸   NM_001256678
- Peptide Label: isoform 2
- UniProtKB: O15091 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243608   ⟸   NM_001256679
- Peptide Label: isoform 3
- UniProtKB: O15091 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243609   ⟸   NM_001256680
- Peptide Label: isoform 4
- UniProtKB: A0A0A0MTQ0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243610   ⟸   NM_001256681
- Peptide Label: isoform 4
- UniProtKB: A0A0A0MTQ0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000454657   ⟸   ENST00000557565
Ensembl Acc Id: ENSP00000450898   ⟸   ENST00000557404
Ensembl Acc Id: ENSP00000324697   ⟸   ENST00000321130
Ensembl Acc Id: ENSP00000440915   ⟸   ENST00000534898
Ensembl Acc Id: ENSP00000474967   ⟸   ENST00000603611
Ensembl Acc Id: ENSP00000473856   ⟸   ENST00000603544
Ensembl Acc Id: ENSP00000474656   ⟸   ENST00000604073
Ensembl Acc Id: ENSP00000474620   ⟸   ENST00000604948
Ensembl Acc Id: ENSP00000474700   ⟸   ENST00000605201
Ensembl Acc Id: ENSP00000474299   ⟸   ENST00000605870
Ensembl Acc Id: ENSP00000250377   ⟸   ENST00000250377
RefSeq Acc Id: NP_001401432   ⟸   NM_001414503
- Peptide Label: isoform 1 precursor
- UniProtKB: Q86YB5 (UniProtKB/Swiss-Prot),   Q86SZ4 (UniProtKB/Swiss-Prot),   O15091 (UniProtKB/Swiss-Prot),   D3DSA1 (UniProtKB/Swiss-Prot),   D3DS99 (UniProtKB/Swiss-Prot),   C4AM93 (UniProtKB/Swiss-Prot),   B4E211 (UniProtKB/Swiss-Prot),   B4E0S8 (UniProtKB/Swiss-Prot),   B4DXD9 (UniProtKB/Swiss-Prot),   Q8N5L5 (UniProtKB/Swiss-Prot)
Protein Domains
PRORP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O15091-F1-model_v2 AlphaFold O15091 1-583 view protein structure

Promoters
RGD ID:6791460
Promoter ID:HG_KWN:19211
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000321130,   OTTHUMT00000276687,   UC001WST.1,   UC001WSU.1,   UC001WSW.2,   UC001WSX.1,   UC001WSY.1,   UC001WSZ.1,   UC001WTA.1,   UC001WTB.1,   UC001WTC.1,   UC010AMN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361434,660,786 - 34,661,662 (+)MPROMDB
RGD ID:7227419
Promoter ID:EPDNEW_H19455
Type:initiation region
Name:KIAA0391_1
Description:KIAA0391
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19456  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,552 - 35,122,612EPDNEW
RGD ID:7227421
Promoter ID:EPDNEW_H19456
Type:initiation region
Name:KIAA0391_2
Description:KIAA0391
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19455  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381435,122,675 - 35,122,735EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19958 AgrOrtholog
COSMIC PRORP COSMIC
Ensembl Genes ENSG00000100890 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000258790 Ensembl
Ensembl Transcript ENST00000250377 ENTREZGENE
  ENST00000250377.11 UniProtKB/Swiss-Prot
  ENST00000321130 ENTREZGENE
  ENST00000321130.14 UniProtKB/Swiss-Prot
  ENST00000534898 ENTREZGENE
  ENST00000534898.9 UniProtKB/Swiss-Prot
  ENST00000557404.3 UniProtKB/TrEMBL
  ENST00000603544.5 UniProtKB/Swiss-Prot
  ENST00000603611.5 UniProtKB/TrEMBL
  ENST00000604073.1 UniProtKB/TrEMBL
  ENST00000604948 ENTREZGENE
  ENST00000604948.5 UniProtKB/Swiss-Prot
  ENST00000605201.1 UniProtKB/TrEMBL
  ENST00000605870 ENTREZGENE
  ENST00000605870.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.25.40.10 UniProtKB/Swiss-Prot
  3.40.50.11980 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000100890 GTEx
  ENSG00000258790 GTEx
HGNC ID HGNC:19958 ENTREZGENE
Human Proteome Map PRORP Human Proteome Map
InterPro MRPP3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRORP_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPR-like_helical_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:9692 UniProtKB/Swiss-Prot
NCBI Gene 9692 ENTREZGENE
OMIM 609947 OMIM
PANTHER PTHR13547:SF1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UNCHARACTERIZED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PRORP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134879499 PharmGKB
UniProt A0A0A0MTQ0 ENTREZGENE, UniProtKB/TrEMBL
  B4DXD9 ENTREZGENE
  B4E0S8 ENTREZGENE
  B4E211 ENTREZGENE
  C4AM93 ENTREZGENE
  D3DS99 ENTREZGENE
  D3DSA1 ENTREZGENE
  MRPP3_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q86SZ4 ENTREZGENE
  Q86YB5 ENTREZGENE
  Q8N5L5 ENTREZGENE
  S4R3S1_HUMAN UniProtKB/TrEMBL
  S4R3T4_HUMAN UniProtKB/TrEMBL
  S4R416_HUMAN UniProtKB/TrEMBL
UniProt Secondary B4DXD9 UniProtKB/Swiss-Prot
  B4E0S8 UniProtKB/Swiss-Prot
  B4E211 UniProtKB/Swiss-Prot
  C4AM93 UniProtKB/Swiss-Prot
  D3DS99 UniProtKB/Swiss-Prot
  D3DSA1 UniProtKB/Swiss-Prot
  Q86SZ4 UniProtKB/Swiss-Prot
  Q86YB5 UniProtKB/Swiss-Prot
  Q8N5L5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-04-16 PRORP  protein only RNase P catalytic subunit  KIAA0391  KIAA0391  Symbol and/or name change 5135510 APPROVED